Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
2026119636
Device Listing 2026119636
Listing Summary
#
Listing key
2026119636
Premarket submission
K051594
Device
MCCARTNEY ACCESS TUBE
Applicant
Gynetech Pty. , Ltd.
Product code
HEW
Decision date
2005-09-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
122106
3008693678
3008693678
Nadege Boursiqout
1
N
2026-01-01
1856 Corporate Dr Ste 135 Norcross GA US 30093